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{
"count": 221304,
"next": "https://panelapp-aus.org/api/v1/activities/?format=api&page=305",
"previous": "https://panelapp-aus.org/api/v1/activities/?format=api&page=303",
"results": [
{
"created": "2025-01-19T19:05:37.364925+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "edited their review of gene: LMNB1: Changed phenotypes: Microcephaly 26, primary, autosomal dominant, MIM# 619179, Global developmental delay, Intellectual disability, Microcephaly, Short stature, Seizures, Abnormality of the corpus callosum, Cortical gyral simplification, Feeding difficulties, Scoliosis, Leukodystrophy, adult-onset, autosomal dominant, MIM# 169500, Leukodystrophy, demyelinating, adult-onset, autosomal dominan, atypical, MIM#621061",
"entity_name": "LMNB1",
"entity_type": "gene"
},
{
"created": "2025-01-17T16:00:28.849184+11:00",
"panel_name": "Fetal anomalies",
"panel_id": 3763,
"panel_version": "1.306",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HYAL2 were changed from Cleft lip and palate; cor triatriatum; congenital cardiac malformations to Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063",
"entity_name": "HYAL2",
"entity_type": "gene"
},
{
"created": "2025-01-17T16:00:09.583638+11:00",
"panel_name": "Clefting disorders",
"panel_id": 3368,
"panel_version": "0.259",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HYAL2 were changed from Cleft lip and palate; cor triatriatum; congenital cardiac malformations to Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063",
"entity_name": "HYAL2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:59:47.784825+11:00",
"panel_name": "Mendeliome",
"panel_id": 137,
"panel_version": "1.2265",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HYAL2 were changed from Cleft lip and palate; cor triatriatum; congenital cardiac malformations to Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063",
"entity_name": "HYAL2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:59:16.361614+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.430",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: HYAL2 were changed from Cleft lip and palate; cor triatriatum; congenital cardiac malformations to Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063",
"entity_name": "HYAL2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:58:38.721452+11:00",
"panel_name": "Congenital Heart Defect",
"panel_id": 76,
"panel_version": "0.429",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: HYAL2: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Muggenthaler-Chowdhury-Chioza syndrome, MIM# 621063; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "HYAL2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:26:16.646316+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAPSS2 as ready",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:26:16.624659+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: papss2 has been classified as Green List (High Evidence).",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:25:52.398832+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.302",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAPSS2 were changed from Brachyolmia 4 with mild epiphyseal and metaphyseal changes 612847 to Brachyolmia 4 with mild epiphyseal and metaphyseal changes MIM#612847",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T15:25:21.453566+11:00",
"panel_name": "Skeletal dysplasia",
"panel_id": 258,
"panel_version": "0.301",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PAPSS2 were set to ",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T12:00:25.332497+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GTF3C3 as Green List (high evidence)",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T12:00:25.318488+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gtf3c3 has been classified as Green List (High Evidence).",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:59:52.354151+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Classified gene: GTF3C3 as Green List (high evidence)",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:59:52.337686+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.102",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gtf3c3 has been classified as Green List (High Evidence).",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:59:43.143896+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: GTF3C3 as ready",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:59:43.129846+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: gtf3c3 has been classified as Red List (Low Evidence).",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:59:09.203422+11:00",
"panel_name": "Genetic Epilepsy",
"panel_id": 202,
"panel_version": "1.101",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: GTF3C3: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Neurodevelopmental disorder MONDO:0700092, GTF3C3-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "GTF3C3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:57:13.963479+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX16 as ready",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:57:13.944858+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex16 has been classified as Green List (High Evidence).",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:57:10.597062+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1235",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX16 were changed from Peroxisome biogenesis disorder 8A, (Zellweger), 614876 to Peroxisome biogenesis disorder 8A (Zellweger) MIM#614876; Peroxisome biogenesis disorder 8B MIM#614877",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:56:57.598295+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1234",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PEX16 were set to ",
"entity_name": "PEX16",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:56:33.495533+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PHYH as ready",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:56:33.481385+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: phyh has been classified as Green List (High Evidence).",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:56:30.484523+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1233",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PHYH were changed from Refsum disease, 266500 (3) to Refsum disease MIM#266500",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:56:18.884048+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1232",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PHYH were set to ",
"entity_name": "PHYH",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:55:45.587721+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIGL as ready",
"entity_name": "PIGL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:55:45.572453+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pigl has been classified as Green List (High Evidence).",
"entity_name": "PIGL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:55:42.257886+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1231",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIGL were changed from CHIME syndrome, 280000 (3) to CHIME syndrome, MIM# 280000, MONDO:0010221",
"entity_name": "PIGL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:55:31.078484+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1230",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIGL were set to ",
"entity_name": "PIGL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:55:16.934989+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "reviewed gene: PIGL: Rating: GREEN; Mode of pathogenicity: None; Publications: 22444671, 31535386, 30023290, 29473937, 28371479, 25706356; Phenotypes: CHIME syndrome, MIM# 280000, MONDO:0010221; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal",
"entity_name": "PIGL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:53:29.433202+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PYROXD1 as ready",
"entity_name": "PYROXD1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:53:29.422259+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pyroxd1 has been classified as Green List (High Evidence).",
"entity_name": "PYROXD1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:53:24.930805+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1229",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PYROXD1 were changed from Myopathy, myofibrillar, 8, 617258 (3), Autosomal recessive to Myopathy, myofibrillar, 8 MIM#617258",
"entity_name": "PYROXD1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:53:09.316580+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1228",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PYROXD1 were set to ",
"entity_name": "PYROXD1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:51:33.025299+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NDUFS2 as ready",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:51:33.016406+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: ndufs2 has been classified as Green List (High Evidence).",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:51:30.060685+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1227",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NDUFS2 were changed from Mitochondrial complex I deficiency, 252010 (3) to Mitochondrial complex I deficiency, nuclear type 6, MIM #618228",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:51:19.111998+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1226",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NDUFS2 were set to ",
"entity_name": "NDUFS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:52.114853+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEU1 as ready",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:52.101523+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: neu1 has been classified as Green List (High Evidence).",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:48.844907+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1225",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEU1 were changed from Sialidosis, type I, 256550 (3) to Sialidosis, type I, MIM #256550; Sialidosis, type II, MIM #256550",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:31.872732+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1224",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEU1 were set to ",
"entity_name": "NEU1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:06.953373+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NEXMIF as ready",
"entity_name": "NEXMIF",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:06.944430+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nexmif has been classified as Green List (High Evidence).",
"entity_name": "NEXMIF",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:50:03.707048+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1223",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NEXMIF were changed from Mental retardation, X-linked 98, MIM #300912 to Intellectual developmental disorder, X-linked 98, MIM #300912",
"entity_name": "NEXMIF",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:49:55.152159+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1222",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NEXMIF were set to ",
"entity_name": "NEXMIF",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:49:14.315510+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: XYLT1 as ready",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:49:14.305069+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: xylt1 has been classified as Green List (High Evidence).",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:49:10.692321+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1221",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: XYLT1 were changed from Desbuquois dysplasia 2, 615777 (3) to Desbuquois dysplasia 2, MIM#615777",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:48:24.522998+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1220",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: XYLT1 were set to ",
"entity_name": "XYLT1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:53.487482+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NSDHL as ready",
"entity_name": "NSDHL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:53.469272+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nsdhl has been classified as Green List (High Evidence).",
"entity_name": "NSDHL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:49.855887+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1219",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NSDHL were changed from CK syndrome, 300831 (3) to CK syndrome, MIM#300831",
"entity_name": "NSDHL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:37.398180+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1218",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: NSDHL were set to ",
"entity_name": "NSDHL",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:11.342322+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PAPSS2 as ready",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:11.317462+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: papss2 has been classified as Green List (High Evidence).",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:47:07.342012+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1217",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PAPSS2 were changed from Brachyolmia 4 with mild epiphyseal and metaphyseal changes, 612847 (3) to Brachyolmia 4 with mild epiphyseal and metaphyseal changes, MIM#612847",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:46:50.915508+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1216",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PAPSS2 were set to ",
"entity_name": "PAPSS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:46:27.110481+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: KRT8 as ready",
"entity_name": "KRT8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:46:27.087718+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: krt8 has been classified as Red List (Low Evidence).",
"entity_name": "KRT8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:46:23.946043+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1215",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: KRT8 were changed from CIRRHOSIS, FAMILIAL, MIM #215600 to Cirrhosis, cryptogenic, MIM#215600",
"entity_name": "KRT8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:45:38.547261+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PDHB as ready",
"entity_name": "PDHB",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:45:38.534499+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pdhb has been classified as Green List (High Evidence).",
"entity_name": "PDHB",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:45:14.846414+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1214",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PDHB were changed from Pyruvate dehydrogenase E1-beta deficiency, 614111 (3) to Pyruvate dehydrogenase E1-beta deficiency, MIM#614111",
"entity_name": "PDHB",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:45:02.258176+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1213",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PDHB were set to ",
"entity_name": "PDHB",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:43:40.091632+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX2 as ready",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:43:40.073990+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex2 has been classified as Green List (High Evidence).",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:43:36.950406+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1212",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX2 were changed from Peroxisome biogenesis disorder 5A (Zellweger), 614866 to Peroxisome biogenesis disorder 5A (Zellweger), MIM#614866; Peroxisome biogenesis disorder 5B, MIM#614867",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:43:25.226146+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1211",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PEX2 were set to ",
"entity_name": "PEX2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:53.466769+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP2 as ready",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:53.456882+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap2 has been classified as Green List (High Evidence).",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:48.815927+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1210",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGAP2 were changed from Hyperphosphatasia with mental retardation syndrome 3, 614207 (3) to Hyperphosphatasia with impaired intellectual development syndrome 3, MIM#614207",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:36.875442+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1209",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGAP2 were set to ",
"entity_name": "PGAP2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:09.919739+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PEX1 as ready",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:09.909495+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pex1 has been classified as Green List (High Evidence).",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:42:06.757927+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1208",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PEX1 were changed from Peroxisome biogenesis disorder 1A (Zellweger), 214100 to Peroxisome biogenesis disorder 1A (Zellweger), MIM#214100",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:41:56.173052+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1207",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PEX1 were set to ",
"entity_name": "PEX1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:41:28.346451+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MFSD8 as ready",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:41:28.328651+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mfsd8 has been classified as Green List (High Evidence).",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:41:25.433000+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1206",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MFSD8 were changed from Ceroid lipofuscinosis, neuronal, 7, 610951 (3) to Ceroid lipofuscinosis, neuronal, 7, MIM# 610951",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:41:11.854765+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1205",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MFSD8 were set to ",
"entity_name": "MFSD8",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:44.580150+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PGAP3 as ready",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:44.568630+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pgap3 has been classified as Green List (High Evidence).",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:41.448895+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1204",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PGAP3 were changed from Hyperphosphatasia with mental retardation syndrome 4, 615716 (3) to Hyperphosphatasia with mental retardation syndrome 4, MIM# 615716, MONDO:0014318",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:29.790118+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1203",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PGAP3 were set to ",
"entity_name": "PGAP3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:04.734115+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MID1 as ready",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:04.710470+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mid1 has been classified as Green List (High Evidence).",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:40:01.548497+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1202",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MID1 were changed from Opitz GBBB syndrome, type I, 300000 (3) to Opitz GBBB syndrome MIM#300000; MONDO:0017138",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:39:49.515771+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1201",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MID1 were set to ",
"entity_name": "MID1",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:39:22.878315+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: MMP21 as ready",
"entity_name": "MMP21",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:39:22.868598+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: mmp21 has been classified as Green List (High Evidence).",
"entity_name": "MMP21",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:39:19.635106+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1200",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: MMP21 were changed from Heterotaxy, visceral, 7, autosomal, 616749 (3), Autosomal recessive to Heterotaxy, visceral, 7, autosomal MIM#616749; MONDO:0014762",
"entity_name": "MMP21",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:39:06.809679+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1199",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: MMP21 were set to ",
"entity_name": "MMP21",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:38:42.041844+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: PIH1D3 as ready",
"entity_name": "PIH1D3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:38:42.032560+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: pih1d3 has been classified as Green List (High Evidence).",
"entity_name": "PIH1D3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:38:38.941115+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1198",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: PIH1D3 were changed from Ciliary dyskinesia, primary, 36, X-linked, 300991 (3), X-linked recessive to Ciliary dyskinesia, primary, 36, X-linked, MIM #300991",
"entity_name": "PIH1D3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:38:27.136770+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1197",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Publications for gene: PIH1D3 were set to ",
"entity_name": "PIH1D3",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:37:58.812826+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Marked gene: NARS2 as ready",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:37:58.802793+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Gene: nars2 has been classified as Green List (High Evidence).",
"entity_name": "NARS2",
"entity_type": "gene"
},
{
"created": "2025-01-17T11:37:54.536213+11:00",
"panel_name": "Prepair 1000+",
"panel_id": 3861,
"panel_version": "1.1196",
"user_name": "Zornitza Stark",
"item_type": "entity",
"text": "Phenotypes for gene: NARS2 were changed from Combined oxidative phosphorylation deficiency 24, 616239 (3) to Combined oxidative phosphorylation deficiency 24 - MIM#616239, MONDO:0014547",
"entity_name": "NARS2",
"entity_type": "gene"
}
]
}